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TCAGGTGGCTGGCAGTGTTGAGAGA[C/T]GCCTGACAATCCAAGATCAGGCTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SLC37A3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SLC37A3 - solute carrier family 37 member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287498.1 | 2102 | UTR 3 | NP_001274427.1 | |||
NM_032295.3 | 2102 | Silent Mutation | GCA,GCG | A,A 433 | NP_115671.1 | |
NM_207113.2 | 2102 | UTR 3 | NP_996996.1 | |||
XM_011516626.2 | 2102 | Silent Mutation | GCA,GCG | A,A 483 | XP_011514928.1 | |
XM_011516627.2 | 2102 | Silent Mutation | GCA,GCG | A,A 467 | XP_011514929.1 | |
XM_017012712.1 | 2102 | UTR 3 | XP_016868201.1 | |||
XM_017012713.1 | 2102 | Silent Mutation | GCA,GCG | A,A 433 | XP_016868202.1 | |
XM_017012714.1 | 2102 | UTR 3 | XP_016868203.1 | |||
XM_017012715.1 | 2102 | UTR 3 | XP_016868204.1 | |||
XM_017012716.1 | 2102 | Silent Mutation | GCA,GCG | A,A 345 | XP_016868205.1 | |
XM_017012717.1 | 2102 | UTR 3 | XP_016868206.1 | |||
XM_017012718.1 | 2102 | Intron | XP_016868207.1 |